Literature DB >> 9804767

The identification of two Drosophila K homology domain proteins. Kep1 and SAM are members of the Sam68 family of GSG domain proteins.

M Di Fruscio1, T Chen, S Bonyadi, P Lasko, S Richard.   

Abstract

Sam68 is a member of a growing family of RNA-binding proteins that contains an extended K homology (KH) domain embedded in a larger domain called the GSG (GRP33, Sam68, GLD1) domain. To identify GSG domain family members, we searched data bases for expressed sequence tags encoding related portions of the Sam68 KH domain. Here we report the identification of two novel Drosophila KH domain proteins, which we termed KEP1 (KH encompassing protein) and SAM. SAM bears sequence identity with mammalian Sam68 and may be the Drosophila Sam68 homolog. We demonstrate that SAM, KEP1, and the recently identified Drosophila Who/How are RNA-binding proteins that are able to self-associate into homomultimers. The GSG domain of KEP1 and SAM was necessary to mediate the RNA binding and self-association. To elucidate the cellular roles of these proteins, SAM, KEP1, and Who/How were expressed in mammalian and Drosophila S2 cells. KEP1 and Who/How were nuclear and SAM was cytoplasmic. The expression of KEP1 and SAM, but not Who/How, activated apoptotic pathways in Drosophila S2 cells. The identification of KEP1 and SAM implies that a large GSG domain protein family exists and helps redefine the boundaries of the GSG domain. Taken together, our data suggest that KEP1 and SAM may play a role in the activation or regulation of apoptosis and further implicate the GSG domain in RNA binding and oligomerization.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9804767     DOI: 10.1074/jbc.273.46.30122

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  23 in total

1.  A role for the GSG domain in localizing Sam68 to novel nuclear structures in cancer cell lines.

Authors:  T Chen; F M Boisvert; D P Bazett-Jones; S Richard
Journal:  Mol Biol Cell       Date:  1999-09       Impact factor: 4.138

2.  Identification of cellular mRNA targets for RNA-binding protein Sam68.

Authors:  Michiyasu Itoh; Izumi Haga; Qing-Hua Li; Jun-ichi Fujisawa
Journal:  Nucleic Acids Res       Date:  2002-12-15       Impact factor: 16.971

3.  Translation repression by GLD-1 protects its mRNA targets from nonsense-mediated mRNA decay in C. elegans.

Authors:  Min-Ho Lee; Tim Schedl
Journal:  Genes Dev       Date:  2004-04-22       Impact factor: 11.361

4.  KHDC1A, a novel translational repressor, induces endoplasmic reticulum-dependent apoptosis.

Authors:  Congli Cai; Jing Liu; Chao Wang; Jinhua Shen
Journal:  DNA Cell Biol       Date:  2012-06-25       Impact factor: 3.311

5.  Phosphorylation status of the Kep1 protein alters its affinity for its protein binding partner alternative splicing factor ASF/SF2.

Authors:  Cécile Robard; Alex Daviau; Marco Di Fruscio
Journal:  Biochem J       Date:  2006-11-15       Impact factor: 3.857

6.  Understanding the binding specificities of mRNA targets by the mammalian Quaking protein.

Authors:  Monika Sharma; Shakshi Sharma; Apoorv Alawada
Journal:  Nucleic Acids Res       Date:  2019-11-18       Impact factor: 16.971

7.  Nuclear translocation controlled by alternatively spliced isoforms inactivates the QUAKING apoptotic inducer.

Authors:  J Pilotte; D Larocque; S Richard
Journal:  Genes Dev       Date:  2001-04-01       Impact factor: 11.361

8.  Identification of in vivo mRNA targets of GLD-1, a maxi-KH motif containing protein required for C. elegans germ cell development.

Authors:  M H Lee; T Schedl
Journal:  Genes Dev       Date:  2001-09-15       Impact factor: 11.361

9.  C. elegans RNA-binding protein GLD-1 recognizes its multiple targets using sequence, context, and structural information to repress translation.

Authors:  Jung H Doh; Yuchae Jung; Valerie Reinke; Min-Ho Lee
Journal:  Worm       Date:  2013-10-01

10.  Cloning and characterization of a novel human STAR domain containing cDNA KHDRBS2.

Authors:  Liu Wang; Jian Xu; Li Zeng; Xin Ye; Qihan Wu; Jianfeng Dai; Chaoneng Ji; Shaohua Gu; Chunhua Zhao; Yi Xie; Yumin Mao
Journal:  Mol Biol Rep       Date:  2002-12       Impact factor: 2.316

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.